Canonical Allele Identifier: CA2697546379

Gene:

Linked Data

• ClinVar Variation Id: 2756478
• ClinVar RCV Id: RCV003536869

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707328A>T , CM000667.2:g.112707328A>T	GRCh38
NC_000005.9:g.112043025A>T , CM000667.1:g.112043025A>T	GRCh37
NC_000005.8:g.112070924A>T	NCBI36
NG_008481.4:g.19808A>T , LRG_130:g.19808A>T